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Validation of a portable fundus camera

Validation of A Portable Fundus Camera Using Upcycled Smartphone as Compared to the Routine Dilated Fundus Evaluation by the Clinicians for Assessing Posterior Segment Diseases - Not applicable

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/09/074124
Enrollment
152
Registered
2024-09-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H578- Other specified disorders of eye and adnexa

Interventions

Intervention1: nil: nil

Sponsors

LabSD Inc
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria for cases Patients with posterior segment pathology who are willing to give informed written consent and fulfil the criteria mentioned below 1. Patient of age =18 years and = 70 years 2. Clear media to facilitate capturing of fundus image, either phakic or pseudophakic 3.Patients who have completed evaluation by respective speciality clinician Inclusion criteria for controls Patients without posterior segment pathology who are willing to give informed written consent and fulfil the criteria mentioned below: 1. Patient of age =18 years and = 70 years 2. Clear media to facilitate capturing of fundus image, either phakic or pseudophakic 3. Patients who have completed evaluation by comprehensive clinician

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
To validate the portable fundus camera using upcycled smartphone (EYELIKE™ digital ophthalmoscope) in diagnosing posterior segment diseases as compared to gold standard dilated fundus examination by the clinicians with indirect ophthalmoscopy.Timepoint: Baseline

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Usha Tejaswini S

Aravind Eye Hospital

ushatejaswini.s@aravind.org09916808738

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026